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中性鱼精蛋白锌(NPH)胰岛素可减轻糖尿病大鼠的记忆损伤。

Neutral Protamine Hagedorn (NPH) insulin attenuates memory impairments in diabetic rats.

作者信息

Andrade Marcelo T, Gomes Camila B, Fernandes Débora O, Melo Bruno P, Moraes Michele M, Almeida Ana F S, Alvarado Laura F J, Pereira Grace S, Guimarães Juliana B, Heyman Elsa, Meeusen Romain, Mendes Thiago T, Soares Danusa D

机构信息

Exercise Physiology Laboratory, School of Physical Education, Physiotherapy and Occupational Therapy, Universidade Federal de Minas Gerais, Av. Antônio Carlos, Belo Horizonte, MG, 662731270-901, Brazil.

Exercise Physiology and Health Laboratory, Universidade Federal da Bahia, Salvador, Brazil.

出版信息

Diabetol Metab Syndr. 2025 Jul 11;17(1):264. doi: 10.1186/s13098-025-01820-7.

Abstract

Cognitive decline is a significant complication of type 1 diabetes (T1D) that substantially affects patients' quality of life. Although previous studies suggest that Neutral Protamine Hagedorn (NPH) insulin may mitigate certain effects of streptozotocin-induced type 1 diabetes (T1D), the impact of NPH on diabetes-related cognitive decline remains unclear. This study evaluated the efficacy of NPH insulin in attenuating spatial, short-term, and long-term memory deficits in T1D rats, assessing their progression at 10, 20, and 30 days following diabetes induction and treatment initiation. Sixteen adult male Wistar rats were randomly assigned into diabetic and non-diabetic groups; T1D was induced using streptozotocin (STZ). Diabetic rats received twice-daily injections of NPH insulin and underwent cognitive assessments using the Novel Object Recognition and Spatial Object Recognition tasks. NPH insulin treatment delayed the progression of memory deficits in T1D rats over the 30-day period. Although memory function was not fully restored, insulin treatment effectively delayed deficits across spatial, short-term, and long-term memory domains. However, despite treatment, T1D rats still exhibited memory impairments, highlighting the complexity of diabetes-associated cognitive decline. These findings suggest that NPH insulin offers partial neuroprotection in T1D rats, underscoring the importance of early and consistent diabetes management to preserve cognitive function. Future research should focus on refining insulin therapy strategies to enhance their effectiveness in preventing and reducing diabetes-associated cognitive impairments.

摘要

认知功能衰退是1型糖尿病(T1D)的一种严重并发症,会严重影响患者的生活质量。尽管先前的研究表明中性鱼精蛋白锌胰岛素(NPH)可能会减轻链脲佐菌素诱导的1型糖尿病(T1D)的某些影响,但NPH对糖尿病相关认知功能衰退的影响仍不明确。本研究评估了NPH胰岛素在减轻T1D大鼠空间、短期和长期记忆缺陷方面的疗效,在糖尿病诱导和治疗开始后的第10、20和30天评估其进展情况。16只成年雄性Wistar大鼠被随机分为糖尿病组和非糖尿病组;使用链脲佐菌素(STZ)诱导T1D。糖尿病大鼠每天接受两次NPH胰岛素注射,并使用新物体识别和空间物体识别任务进行认知评估。在30天的时间里,NPH胰岛素治疗延缓了T1D大鼠记忆缺陷的进展。尽管记忆功能没有完全恢复,但胰岛素治疗有效地延缓了空间、短期和长期记忆领域的缺陷。然而,尽管进行了治疗,T1D大鼠仍表现出记忆障碍,凸显了糖尿病相关认知功能衰退的复杂性。这些发现表明,NPH胰岛素在T1D大鼠中提供了部分神经保护作用,强调了早期和持续的糖尿病管理对维持认知功能的重要性。未来的研究应专注于完善胰岛素治疗策略,以提高其预防和减少糖尿病相关认知障碍的有效性。

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